Midgut morphological changes and autophagy during metamorphosis in sand flies.

During metamorphosis, holometabolous insects undergo significant remodeling of their midgut and become able to cope with changes in dietary requirements between larval and adult stages. At this stage, insects must be able to manage and recycle available food resources in order to develop fully into adults, especially when no nutrients are acquired from the environment. Autophagy has been previously suggested to play a crucial role during metamorphosis of the mosquito. Here, we investigate the overall morphological changes of the midgut of the sand fly during metamorphosis and assess the expression profiles of the autophagy-related genes ATG1, ATG6, and ATG8, which are associated with various steps of the autophagic process. Morphological changes in the midgut start during the fourth larval instar, with epithelial degeneration followed by remodeling via the differentiation of regenerative cells in pre-pupal and pupal stages. The changes in the midgut epithelium are paired with the up-regulation of ATG1, ATG6 and ATG8 during the larva-adult transition. Vein, a putative epidermal growth factor involved in regulating epithelial midgut regeneration, is also up-regulated. Autophagy has further been confirmed in sand flies via the presence of autophagosomes residing within the cytoplasmic compartment of the pupal stages. An understanding of the underlying mechanisms of this process should aid the future management of this neglected tropical vector.

Effects of specific antisera targeting peritrophic matrix-associated proteins in the sand fly vector Phlebotomus papatasi.

In many hematophagous insects, the peritrophic matrix (PM) is formed soon after a blood meal (PBM) to compartmentalize the food bolus. The PM is an important component of vector competence, functioning as a barrier to the development of many pathogens including parasites of the genus Leishmania transmitted by sand flies. PM morphology and permeability are associated with the proteins that are part of the PM scaffolding, including several peritrophins, and chitin fibers. Here, we assessed the effects of specific antisera targeting proteins thought to be an integral part of the PM scaffolding and its process of maturation and degradation. Phlebotomus papatasi sand flies were fed with red blood cells reconstituted with antisera targeting the chitinase PpChit1, and the peritrophin PpPer2. Sand fly midguts were dissected at different time points and processed for light microscopy (LM), confocal and transmission electron (TEM) microscopies (24, 42-46, 48 and 72h PBM), scanning electron (SEM) (48h PBM) and atomic force (AFM) (30h PBM) microscopies. TEM and WGA-FITC staining indicate PM degradation was significantly delayed following feeding of flies on anti-PpChit1. AFM analysis at 30h PBM point to an increase in roughness' amplitude of the PM of flies that fed on either anti-PpChit1 or anti-PpPer2. Collective, our data suggest that antibodies targeting PM-associated proteins affects the kinetics of PM maturation, delaying its degradation and disruption and are potential targets on transmission-blocking vaccines strategies.

Seasonal patterns of parasitism of the tropical spiders Theridion evexum (Araneae, Theridiidae) and Allocyclosa bifurca (Araneae, Araneidae) by the wasps Zatypota petronae and Polysphincta gutfreundi (Hymenoptera, Ichneumonidae)

The rates of parasitism of Theridion evexum by the parasitoid wasp Zatypota petronae, and Allocyclosa bifurca by Polysphincta gutfreundi, were followed for two years. Parasitism of T. evexum was very low (mean 1.39+1.8%), and restricted to nearly seven months of the year. Parasitism of A. bifurca was higher (mean 7.8+7.6%), and did not show a seasonal pattern. Reproduction of the host spider T. evexum was highly seasonal, with only one, highly coordinated generation per year, while adults of A. bifurca were present year round. Short-term autocorrelation on parasitism rates over time at different sites suggest that P. gutfreundi tend to return to the same sites to hunt hosts over periods of a few weeks. Rev. Biol. Trop. 56 (2): 749-754. Epub 2008 June 30.

Las tasas de parasitismo de Theridion evexum por la avispa parasitoide Zatypota petronae y de Allocyclosa bifurca por Polysphincta gutfreundi fueron estudiadas durante dos años. El parasitismo en T. evexum fue muy bajo (promedio 1.39+1.8%) y restringido a aproximadamente siete meses del año. El parasitismo en A. bifurca fue más alto (promedio 7.8+7.6%) y no mostró un claro patrón estacional. La reproducción de la araña hospedera T. evexum fue muy estacional, con solamente una generación por año, mientras que los adultos de A. bifurca estuvieron presentes todo el año. Autocorrelaciones de las tasas de parasitismo entre censos consecutivos en diferentes sitios sugiere que P. gutfreundi tiende a retornar a los mismos sitios para parasitar las arañas hospederas durante algunas semanas.

Seasonal patterns of parasitism of the tropical spiders Theridion evexum (Araneae, Theridiidae) and Allocyclosa bifurca (Araneae, Araneidae) by the wasps Zatypota petronae and Polysphincta gutfreundi (Hymenoptera, Ichneumonidae).

The rates of parasitism of Theridion evexum by the parasitoid wasp Zatypota petronae, and Allocyclosa bifurca by Polysphincta gutfreundi, were followed for two years. Parasitism of T. evexum was very low (mean 1.39 +/- 1.8%), and restricted to nearly seven months of the year. Parasitism of A. bifurca was higher (mean 7.8 +/- 7.6%), and did not show a seasonal pattern. Reproduction of the host spider T evexum was highly seasonal, with only one, highly coordinated generation per year, while adults of A. bifurca were present year round. Short-term autocorrelation on parasitism rates over time at different sites suggest that P. gutfreundi tend to return to the same sites to hunt hosts over periods of a few weeks.

Tie them up tight: wrapping by Philoponella vicina spiders breaks, compresses and sometimes kills their prey.

We show that uloborid spiders, which lack the poison glands typical of nearly all other spiders, employ thousands of wrapping movements with their hind legs and up to hundreds of meters of silk line to make a shroud that applies substantial compressive force to their prey. Shrouds sometimes break the prey's legs, buckle its compound eyes inward, or kill it outright. The compressive force apparently results from the summation of small tensions on sticky lines as they are applied to the prey package. Behavioral details indicate that wrapping is designed to compact prey; in turn, compaction probably functions to facilitate these spiders' unusual method of feeding. This is the first demonstration that prey wrapping by spiders compacts and physically damages their prey, rather than simply restraining them.